Kinetic Surgical, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Kinetic Surgical, LLC makes
Kinetic Surgical, LLC manufactures the MARIONETTE SA robotic surgical system (models 001 001 and 001 002) and the STATARIUS surgical accessory (model 001 003), designed for minimally invasive procedures.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
Marionette SA, Model 001 001 & 001 002 Ref K072811
Regimes: 510(k) Registry: 510(k)Statarius, Model 001 003 Ref K061292
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kinetic Surgical, LLC have in the registry?
The registry currently lists 2 devices for Kinetic Surgical, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kinetic Surgical, LLC's devices?
Among its 2 most recently registered devices, Kinetic Surgical, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Kinetic Surgical, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Kinetic Surgical, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kinetic Surgical, LLC in the registry?
The most recently registered devices listed for Kinetic Surgical, LLC include MARIONETTE SA, MODEL 001 001 & 001 002 and STATARIUS, MODEL 001 003.